Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Fig. 3.

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Fig. 3. Diagnostic workflow for patients with INS. Traditionally, patients would receive numerous investigations before the identification of the underlying etiology. The new pathway using targeted gene panel sequencing as a frontline diagnostic tool would provide genotype-driven tailored investigation. This pathway will help patients avoid unnecessary examinations or treatments. INS, infantile nystagmus syndrome.
Journal of Genetic Medicine 2024;21:14-21
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